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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Mutagenic activity of the glutathione S-transferase substrate 1-chloro-2,4-dinitrobenzene (CDNB) in the Salmonella mutagenicity assay.
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Mutagenic activity of the glutathione S-transferase substrate 1-chloro-2,4-dinitrobenzene (CDNB) in the Salmonella mutagenicity assay.

机译:沙门氏菌诱变性测定中谷胱甘肽S-转移酶底物1-氯-2,4-二硝基苯(CDNB)的诱变活性。

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摘要

The mutagenicity of the commonly used glutathione S-transferase substrates 1-chloro-2,4-dinitrobenzene (CDNB) and 1,2-dichloro-4-nitrobenzene (DCNB) was investigated in the Salmonella mutagenicity assay. CDNB induced a concentration-dependent mutagenic response in Salmonella typhimurium strain TA98. Incorporation of an activation system derived from Aroclor 1254-induced rats did not influence mutagenic response. Under the same conditions DCNB failed to display mutagenic activity. The mutagenic activity of CDNB was attenuated in bacterial strains under-expressing nitroreductase or O-acetylase activity but, in contrast, it was exaggerated in an O-acetylase over-expressing strain. It is inferred that CDNB exhibits a mutagenic response following reduction of the nitro-group to the hydroxylamine, which is further acetylated to form the acetoxy derivative that presumably breaks down spontaneously to generate the nitrenium ion, the likely ultimate mutagen.
机译:在沙门氏菌诱变性测定中研究了常用的谷胱甘肽S-转移酶底物1-氯-2,4-二硝基苯(CDNB)和1,2-二氯-4-硝基苯(DCNB)的致突变性。 CDNB在鼠伤寒沙门氏菌TA98菌株中诱导了浓度依赖性诱变反应。引入源自Aroclor 1254诱导的大鼠的激活系统不会影响诱变反应。在相同条件下,DCNB无法显示诱变活性。 CDNB的诱变活性在表达量不足的硝基还原酶或O-乙酰化酶活性较低的细菌菌株中减弱,但是相反,在表达O-乙酰化酶的过表达菌株中则夸大了。可以推断,在硝基还原为羟胺后,CDNB表现出诱变反应,羟胺进一步被乙酰化以形成乙酰氧基衍生物,该乙酰氧基衍生物可能自发分解生成nitr离子,可能是最终的诱变剂。

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